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NuVasive Receives FDA 510(k) Clearance to Market MAGEC System -

NuVasive Specialized Orthopedics received FDA 510(k) clearance to market the MAGEC® system for implantation via the Reline® posterior fixation system to treat severe spinal deformity.

MAGEC received its first 510(k) clearance under Ellipse Technologies, in 1Q14. NuVasive acquired Ellipse earlier in 2016. Reline is integrated into NuVasive's Integrated Global Alignment (iGA™) platform, launched in 2015.

Sources: NuVasive, Inc.; ORTHOWORLD Inc.

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